Disease #00707 (MKS8 (Meckel syndrome, type 8 (MKS-8)), OMIM:613885)

Official abbreviation MKS8
Name Meckel syndrome, type 8 (MKS-8)
OMIM ID 613885
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TCTN2
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.